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Recent Developments in Cross-Coupling Reactions

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Organic Chemistry".

Deadline for manuscript submissions: 31 October 2024 | Viewed by 183

Special Issue Editors


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Guest Editor
Department of Hematology/Oncology, University of Virginia, Charllotesville, VA 22903, USA
Interests: cross-coupling reactions; heterogeneous catalysts; bio-active compounds; asymmetric synthesis; organometallic chemistry; green chemistry; nanocatalysis; synthetic methodologies

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Guest Editor
Indian Institute of Chemical Technology, Tarnaka, Hyderabad, TS 500007, India
Interests: synthetic methodologies; green chemistry; biomimetic chemistry; organometallic chemistry; nanocatalysis

Special Issue Information

Dear Colleagues,

Cross-coupling reactions are reactions in organic chemistry in which two different fragments are combined with the help of a metal catalyst to form a product. For instance, R-M, where R is an organic fragment and M is a main group center, reacts with an organic halide (R1-X) to produce a new carbon–carbon bond. This protocol is used in the majority of arylations. These are used to form carbon–carbon and carbon–heteroatom bonds (C-C and C-X, respectively).

In addition, the importance of cross-coupling reactions using catalysts based on transition metals is significant in methodologies that use heterogeneous catalysis, as they play a fundamental role in the production of important compounds in the pharmaceutical industry as well as polymers. In 2010, Akira Suzuki, Ei-ichi Negishi, and Richard F. Heck were awarded a Nobel Prize in Chemistry for their work on palladium-catalyzed cross-coupling reactions.

Moreover, catalysts such as palladium and palladium-supported catalysts are frequently useful in the formation of carbon–carbon and carbon–heteroatom bonds due to their high functional group tolerance. These catalysts are also stable at elevated temperatures, in water, and in air. Many researchers around the globe would like to develop coupling reactions with minimal metal traces in the products. In addition, palladium-based catalysts are becoming more common in organic chemistry for the formation of C-C and C-heteroatom (C-X) bonds.

Dr. Ramesh Katla
Dr. Y. V. D. Nageswar
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Molecules is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • cross-coupling reactions
  • C-S cross-coupling reactions
  • C-Se cross-coupling reactions
  • C-N cross-coupling reactions
  • C-O cross-coupling reactions
  • microwave-mediated cross-coupling reactions
  • metal-catalyzed reactions

Published Papers

This special issue is now open for submission.
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